Two cousins with neonatal stroke, PAI-1 4G variant and MTHFR A1298C mutation
Meredith R Golomb1, Mark Heiny, Bhuwan P Garg
1Division of Pediatric Neurology, Department of Neurology, Indiana University School of Medicine, Indianapolis 46202, USA. mgolomb@iupui.edu
Abstract:
The authors describe 2 female cousins with neonatal stroke. One was heterozygous for the plasminogen activator inhibitor-1 4G variant and compound heterozygous for the A1298C and C677T methylenetetrahydrofolate reductase mutations. Her cousin was homozygous for the plasminogen activator inhibitor-1 4G variant and heterozygous for the methylenetetrahydrofolate reductase A1298C and factor V Leiden mutations.
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